AU7418100A - Method for producing (r) or (s)-hydroxy-gamma-butyrolactone - Google Patents
Method for producing (r) or (s)-hydroxy-gamma-butyrolactoneInfo
- Publication number
- AU7418100A AU7418100A AU74181/00A AU7418100A AU7418100A AU 7418100 A AU7418100 A AU 7418100A AU 74181/00 A AU74181/00 A AU 74181/00A AU 7418100 A AU7418100 A AU 7418100A AU 7418100 A AU7418100 A AU 7418100A
- Authority
- AU
- Australia
- Prior art keywords
- butyrolactone
- gamma
- hydroxy
- producing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D307/30—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/32—Oxygen atoms
- C07D307/33—Oxygen atoms in position 2, the oxygen atom being in its keto or unsubstituted enol form
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP99117685 | 1999-09-08 | ||
EP99117685 | 1999-09-08 | ||
US18536600P | 2000-02-28 | 2000-02-28 | |
US60185366 | 2000-02-28 | ||
PCT/EP2000/008810 WO2001018231A2 (de) | 1999-09-08 | 2000-09-08 | VERFAHREN ZUR HERSTELLUNG VON (R)- ODER (S)-HYDROXY-η-BUTYROLACTON |
Publications (1)
Publication Number | Publication Date |
---|---|
AU7418100A true AU7418100A (en) | 2001-04-10 |
Family
ID=26153103
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU74181/00A Abandoned AU7418100A (en) | 1999-09-08 | 2000-09-08 | Method for producing (r) or (s)-hydroxy-gamma-butyrolactone |
Country Status (2)
Country | Link |
---|---|
AU (1) | AU7418100A (de) |
WO (1) | WO2001018231A2 (de) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2003250323A1 (en) * | 2002-08-22 | 2004-03-11 | Neurosearch A/S | A method of preparing enantiomers of indole-2,3-dione-3-oxime derivatives |
US11247976B2 (en) | 2016-04-29 | 2022-02-15 | Wisconsin Alumni Research Foundation | Synthetic ligands that modulate the activity of the RhlR quorum sensing receptor |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2542941B2 (ja) * | 1990-02-02 | 1996-10-09 | チッソ株式会社 | 光学活性ヒドロキシラクトン類の製造方法 |
JP2939646B2 (ja) * | 1990-07-17 | 1999-08-25 | チッソ株式会社 | 4―置換―2―ヒドロキシブタン酸エステルおよび製造法 |
JP4196470B2 (ja) * | 1999-03-09 | 2008-12-17 | チッソ株式会社 | 光学活性α−ヒドロキシラクトン類の製造方法 |
-
2000
- 2000-09-08 AU AU74181/00A patent/AU7418100A/en not_active Abandoned
- 2000-09-08 WO PCT/EP2000/008810 patent/WO2001018231A2/de active Application Filing
Also Published As
Publication number | Publication date |
---|---|
WO2001018231A3 (de) | 2001-09-13 |
WO2001018231A2 (de) | 2001-03-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MK6 | Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase |